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Vyaire Medical, Inc. Recalls the Twin Tube Due to The Potential of The Nozzle Separating During Patient Use
Vyaire Medical, Inc. is recalling the Twin Tube due to the potential of the nozzle separating during patient use. The separated component may fall into the patient’s mouth resulting in a potential choking hazard which may lead to an airway obstruction, requiring medical intervention to prevent further injury or harm.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Questions?
If you have questions about this recall, contact Vyaire Medical, Inc. at GMBEMEA‐FSCA‐RDX‐INTL@Vyaire.com.
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